Development and Validation of Uv-Spectrophotometric Method for Estimation of Abacavir Sulfate Nanoparticles.

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* Corresponding author: I.Sowkar Baig.
E-mail address: sowkar79@gmail.com
IJPAR |Volume 2 | Issue 3 | July-Sep - 2013 ISSN: 2320-2831
Available Online at: www.ijpar.com
[Research article]
DEVELOPMENT AND VALIDATION OF UV-SPECTROPHOTOMETRIC
METHOD FOR ESTIMATION OF ABACAVIR SULFATE
NANOPARTICLES.
*1
I.Sowkar Baig, 2
T.Vetricheivan .
1*
Department of Pharmaceutics, Sri Venkateswara College of Pharmacy, R.V.S. Nagar,
Chittoor, A.P.
2
Department of Pharmaceutical Analysis, Adhiparasakthi College of Pharmacy,
Melmaruvathur, Kanchipuram District, Tamil Nadu, India.
ABSTRACT
A simple, precise and accurate spectrophotometric method has been developed for the determination of
Abacavir Sulfate nanoparticles. Standard Stock solution was prepared in pH 7.4 phosphate buffer and further
dilution were carried out with the same. The λmax of Abacavir Sulfate nanoparticles was found to be 285 nm.
The A (1%, 1cm) Value of Abacavir Sulfate nanoparticles was found to be 434. The correlation co efficient (r)
was found to be 0.9999. The limit of detection (LOD) and limit of Quantification (LOQ) was found to be 0.1074
μg/ml and 0.3257 μg/ml respectively for Abacavir Sulfate nanoparticles. The result of estimation in Abacavir
sulfate nanoparticles was found to be 99.62 ± 0.25%. The method was then validated statistically as per KH
guidelines, which yielded good results concerning range, linearity, precision, accuracy specifically, Robustness
and Ruggedness.
KEYWORDS: Abacavir Sulfate, Nanoparticles, Spectrophotometry estimation.
INTRODUCTION
Abacavir Sulfate is a nucleoside reverse
transcriptase inhibitor (nrti) with activity against
Human Immuno deficiency virus type 1 (HIV-1)
and it is chemically {(S, 4R)-4-[2-amino-6-
(Cyclopropylamino) 9H-purine-ayl] cyclopent-2-
enyl} methanol Sulphate. There are number of
analytical methods have been evoked for the
estimation of Abacavir Sulfate either individually
or combination with other antiviral agents in
HPLC, literature survey didn’t reveal any
spectrophotometric method for estimation of
Abacavir Sulfate nanoparticles, In this present
investigation to develop a simple, rapid, precise
and accurate, Robustness and Rugged of Abacavir
sulfate nanoparticles.
Materials and Methods
Pure drug as obtained from Ranbaxy Chemical
Guargon (India) as a gift sample pH 7.4 phosphate
buffer are used entire the experiments. Shimadzu
1700, a double beam UV- spectrophotometer with
1cm matched Quartz cell were used for the
measurement of absorbance. Shimadzu electronic
balance was used for weighing the samples.

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Procedure
Preparation of standard solution (500 μg/ml) was
prepared in ph 7.4 phosphate suffer. From the stock
solution, working standard solution (10 ms/ml) was
prepared by appropriate dilution with ph 7.4
phosphate buffer was determination of λmax and a
(1% 1 cm) value. Working standard solution of
Abacavir sulfate nanoparticles was scanned in the
entire UV range of 200-400nm. The stability
studies data were recovered at 1 hr 80 min. the
λmax and (A1% 1cm) of Abacavir sulfate
nanoparticles were found to be 285 nm and 434
respectively.
Preparation of calibration curve
Standard stock solution prepared in pH 7.4
phosphate buffer to obtained concentration ranging
from 5-30 μg/ml. Absorbance of this solution were
measured at 285 nm. Absorbance was plotted was
plotted versus concentration to obtained calibration
graph. From the calibration curve, the linearity
range was found to out and LOD and LOQ values.
Analysis of the Nanoparticles formulations
Ten Capsules were weighted and average weight
was determined. The average weight were found
and remove the capsule shell and the powdered
nanoparticles equivalent to among of Abacavir
Sulfate into a 50ml volumetric flask, added 10ml of
pH 7.4 phosphate buffer and sonicated for 15 min,
then shaken vigorously for few min and produced
to 50 ml with pH 7.4 phosphate buffer and filtered
through Whatmann’s filter paper No.41. from the
filtrate, pipetted out 3 ml and transferred into 50 ml
flask in some directions for six times.
Recovery studies
To the pre analyzed sample with excipients, a
known quantity of standard solution was added.
The content were mixed, finally made up to the
volume with pH 7.4 phosphate buffer. Absorbance
was measured at 274 nm and the amount present
was calculated by using the slope and intercept.
Limit of Detection (LOD) and Limit of
Quantification (LOQ)
Preparation of Calibration curve from the serial
dilution of the standard was repeated for six times,
the limit of detection and limit of Quantification
was calculated by using the average values of
slopes and standard deviations of intercept.
Repeatability
Repeatability is performed by inter day and intra
day precision analysis. The assay and recovery
procedures were repeated for three times on the
some day and one time on three successive days.
Results and Discussion
The λmax of Abacavir Sulfate nanoparticles was
found to be 234 nm from is spectrum. The A (1%
1cm) value was found to be 434 nm Abacavir
Sulfate nanoparticles showed linear absorption
from 5- 30 μg/ml. The correlation co efficient (r)
was found to be 0.9999. The LOD and LOQ values
were determined from the slope of linearity plot
and standard derivation of y-intercept and found to
be 0.1074μg/ml and 0.3257μg/ml respectively. The
optical characteristics like correlation coefficient,
slope, intercept, Sandell’s sensitivity, LOD and
LOQ were calculated.
Those are shown in Table. 1. The stability of
solutions of formulations was determined by
measuring the absorbance at 284nm at periodic
intervals. There was no considerable change in the
absorbance at this wave length up to 1hr 20 mins
indicating that the solutions was stable for at least
1hr 20mins. The nanoparticles formulations were
carried out and the mean assay values was found to
be 99.62±0.25%. These are shown in Table 2.
The corresponding RSD values were found to be
0.76% indicating that the method has required
precision. The accuracy of the Method was
determined by recovery studies. The Mean
recovery for Abacavir sulfate nanoparticles was
found to be 100.38 ± 0.29% indicating that the
method has required accuracy. The validation
results are given in Table -3.
A new analytical method was developed and
validated. The estimation of Abacavir Sulfate
nanoparticles was achieved by U.V. method, after
considering the solubility and stability, phosphate
buffer pH 7.4 was selected as solvent and the
284nm was selected wave length for analysis.

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Table 1: Optical characteristics of Abacavir sulfate by UV Spectroscopic method
S.NO PARAMETERS METHOD
1  max (nm) 285
2 Beers law limit (µg/ml) 4-24
3 Correlation coefficient (r)* 0.9999
4 Regression equation (y=mx+c) 0.04709+0.0002797
5 Slope (m) 0.04709
6 Intercept (c) 0.0002797
7 LOD (µg/ml) 0.1074
8 LOQ (µg/ml) 0.3257
9
Sandell’s sensitivity
(µg/cm2
/0.001 A.U)
0.021313
10 Standard Error of Mean 0.003886
*Average of six determinations
Table 2: Quantification of formulation - (Abacavir sulfate)
S.No Labeled
Amount (mg)
Amount
Found (mg)
Percentage
Obtained (%)
Percentage
Found*
S.D. (+/-
)
%
R.S.D
S.E
1 50 49.93 99.87 99.62% 0.769225 0.77218 0.021367
2 50 50.25 100.51
3 50 48.09 98.18
4 50 49.83 99.66
5 50 49.87 99.74
6 50 49.87 99.74
* Average of Six determinations
Table 3: Recovery studies for formulation - (Abacavir sulfate)
S.No
Amount
Present
(µg/ml)
Amount
Added
(µg/ml)
Amount
Estimated
(µg/ml)
Amount
recovered
(µg/ml)
Percentage
recovered
(%)
Average
percentage
recovery*
1 12.45 2 14.47 2.02 101
100.38%2 12.45 4 16.39 3.94 98.50
3 12.45 6 18.48 6.03 100.50
4 12.45 8 20.52 8.07 100.80
5 12.45 10 22.55 10.05 100.50
6 12.45 12 24.58 12.13 101.08
* Values are mean of Six observations

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Conclusion
Thus, the development method is simple, accurate,
precise and cost effective. Hence, it can be used for
routine analysis of Abacavir sulfate nanoparticles
in pharmaceutical preparation.
Acknowledgements
To our sincere thanks to Ranbaxy, chemicals
Guargon (India). For providing gift sample of pure
Abacavir Sulfate. We also extend our Thanks to
Principal and H.O.D, Department of
Pharmaceutical Analysis research from
Adhiparasakthi College of Pharmacy for providing
the necessary facilities.
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